Rs. Goldstein et al., IN-VIVO NGF TREATMENT INCREASES PROLIFERATION IN THE PRIMARY SYMPATHETIC-GANGLIA OF CHICK-EMBRYOS, Developmental biology, 181(1), 1997, pp. 116-120
Nerve growth factor (NGF) is considered to be a target-derived surviva
l or differentiation factor for neural crest cells of the sympathoadre
nal lineage. However, exogenous NGF was found to have a positive effec
t on the size of the primary sympathetic ganglia (PSG) of the chick em
bryo, well before sympathetic innervation of the periphery. We have de
termined the cellular mechanism of NGF's action on the PSG by quantify
ing both proliferation and apoptosis. The proportion of PSG cells in S
-phase is nearly double in NGF-treated embryos compared to that in con
trols, strongly suggesting that NGF acts as a mitogenic factor. NGF re
duced the low level of apoptosis at this stage as well. Since trkA has
not been detected in the avian sympathetic ganglia until later in dev
elopment, we suggest that these early effects of exogenous NGF may be
mediated by the low-affinity neurotrophin receptor, p75, which is expr
essed from neural crest migration stages. (C) 1997 Academic Press